Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP245838.RAAWD0LjvO9EIJwrTr0xVoRCidN1bnB23d2yFyqGT9tSo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP245838.RAAWD0LjvO9EIJwrTr0xVoRCidN1bnB23d2yFyqGT9tSo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP245838.RAAWD0LjvO9EIJwrTr0xVoRCidN1bnB23d2yFyqGT9tSo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP245838.RAAWD0LjvO9EIJwrTr0xVoRCidN1bnB23d2yFyqGT9tSo130_provenance.
- NP245838.RAAWD0LjvO9EIJwrTr0xVoRCidN1bnB23d2yFyqGT9tSo130_assertion description "[Although autosomal dominant polycystic kidney disease type 2 (PKD2) is known to have a milder clinical phenotype than PKD1, neither disorder has been compared with an unaffected control population in terms of survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP245838.RAAWD0LjvO9EIJwrTr0xVoRCidN1bnB23d2yFyqGT9tSo130_provenance.
- NP245838.RAAWD0LjvO9EIJwrTr0xVoRCidN1bnB23d2yFyqGT9tSo130_assertion evidence source_evidence_literature NP245838.RAAWD0LjvO9EIJwrTr0xVoRCidN1bnB23d2yFyqGT9tSo130_provenance.
- NP245838.RAAWD0LjvO9EIJwrTr0xVoRCidN1bnB23d2yFyqGT9tSo130_assertion SIO_000772 10023895 NP245838.RAAWD0LjvO9EIJwrTr0xVoRCidN1bnB23d2yFyqGT9tSo130_provenance.
- NP245838.RAAWD0LjvO9EIJwrTr0xVoRCidN1bnB23d2yFyqGT9tSo130_assertion wasDerivedFrom befree-2016 NP245838.RAAWD0LjvO9EIJwrTr0xVoRCidN1bnB23d2yFyqGT9tSo130_provenance.
- NP245838.RAAWD0LjvO9EIJwrTr0xVoRCidN1bnB23d2yFyqGT9tSo130_assertion wasGeneratedBy ECO_0000203 NP245838.RAAWD0LjvO9EIJwrTr0xVoRCidN1bnB23d2yFyqGT9tSo130_provenance.
- befree-2016 importedOn "2016-02-19" NP245838.RAAWD0LjvO9EIJwrTr0xVoRCidN1bnB23d2yFyqGT9tSo130_provenance.